Shihui Yu
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
-
- Prenatal Screening and Diagnostics
Papers in
-
- Congenital heart defects research 7
- Genetics 18
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 3
- Chronic Lymphocytic Leukemia Research 2
- Co-authors
- Douglas C. Bittel (7 shared papers)W. Graf (5 shared papers)Stephanie D. Fiedler (4 shared papers)David L. Zwick (2 shared papers)Nataliya Kibiryeva (5 shared papers)Julie M. Joyce (2 shared papers)Arivudainambi Ramalingam (1 shared paper)Hongyu Liu (1 shared paper)
- Journals
- PLoS ONE (4 papers)European Journal of Human Genetics (2 papers)Journal of Clinical Medicine (1 paper)Frontiers in Cell and Developmental Biology (1 paper)Current Opinion in Pediatrics (1 paper)
- Partner nations
- ChinaUnited StatesRussia
In The Last Decade
Shihui Yu
30 papers receiving 604 citations
Peers
Comparison fields: 5 of 81
- Genetics 346
- Pediatrics, Perinatology and Child Health 98
- Molecular Biology 326
- Cancer Research 49
- Pulmonary and Respiratory Medicine 101
Countries citing papers authored by Shihui Yu
This map shows the geographic impact of Shihui Yu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Shihui Yu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shihui Yu more than expected).
Fields of papers citing papers by Shihui Yu
This network shows the impact of papers produced by Shihui Yu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Shihui Yu. The network helps show where Shihui Yu may publish in the future.
Co-authors
The 25 scholars most cited alongside Shihui Yu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 97 | |
| 2 | 2006 | 61 | |
| 3 | 2010 | 47 | |
| 4 | 2010 | 46 | |
| 5 | 2015 | 33 | |
| 6 | 2009 | 33 | |
| 7 | 2010 | 32 | |
| 8 | 2012 | 30 | |
| 9 | A 556 kb deletion in the downstream region of the PAX6 gene causes familial aniridia and other eye anomalies in a Chinese family. | 2011 | 27 |
| 10 | 2021 | 27 | |
| 11 | 2010 | 26 | |
| 12 | 2009 | 25 | |
| 13 | 2011 | 19 | |
| 14 | 2021 | 17 | |
| 15 | 2013 | 16 | |
| 16 | 2010 | 15 | |
| 17 | 2012 | 14 | |
| 18 | 2011 | 14 | |
| 19 | 2014 | 11 | |
| 20 | 1993 | 9 |
About Shihui Yu
Shihui Yu is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Physiology and Pulmonary and Respiratory Medicine, having authored 34 papers that have together received 627 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (7 papers), Prenatal Screening and Diagnostics (5 papers), Chromosomal and Genetic Variations (4 papers), Cancer Genomics and Diagnostics (3 papers), Tuberous Sclerosis Complex Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Chronic Lymphocytic Leukemia Research (2 papers). The work is most often cited by research in Genetics (346 citations), Pediatrics, Perinatology and Child Health (98 citations), Molecular Biology (326 citations), Cancer Research (49 citations) and Pulmonary and Respiratory Medicine (101 citations). Shihui Yu has collaborated with scholars based in China, United States and Russia. Frequent co-authors include Douglas C. Bittel, W. Graf, Stephanie D. Fiedler, David L. Zwick, Nataliya Kibiryeva, Julie M. Joyce, Arivudainambi Ramalingam, Hongyu Liu, Linda D. Cooley and Lei Shao. Their work appears in journals such as PLoS ONE, European Journal of Human Genetics, Journal of Clinical Medicine, Frontiers in Cell and Developmental Biology and Current Opinion in Pediatrics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.